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rs762065937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762065937(C;T)
Make rs762065937(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position215064204
GeneABCA12
is asnp
is mentioned by
dbSNPrs762065937
dbSNP (classic)rs762065937
ClinGenrs762065937
ebirs762065937
HLIrs762065937
Exacrs762065937
Gnomadrs762065937
Varsomers762065937
LitVarrs762065937
Maprs762065937
PheGenIrs762065937
Biobankrs762065937
1000 genomesrs762065937
hgdprs762065937
ensemblrs762065937
geneviewrs762065937
scholarrs762065937
googlers762065937
pharmgkbrs762065937
gwascentralrs762065937
openSNPrs762065937
23andMers762065937
23andMe allrs762065937
SNPshotrs762065937
SNPdbers762065937
MSV3drs762065937
GWAS Ctlgrs762065937
Max Magnitude0
ClinVar
Risk rs762065937(G;G) rs762065937(T;T)
Alt rs762065937(G;G) rs762065937(T;T)
Reference Rs762065937(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ABCA12
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.215928927C>G
CLNSRC
CLNACC RCV000256128.1,